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佛波酯刺激后粒细胞集落刺激因子(G-CSF)和粒细胞/巨噬细胞集落刺激因子(GM-CSF)mRNA的表达

Expression of granulocyte colony stimulating factor (G-CSF) and granulocyte/macrophage colony stimulating factor (GM-CSF) mRNA upon stimulation with phorbol ester.

作者信息

Kothari S S, Abrahamsen M S, Cole T, Hammond W P

机构信息

Hope Heart Institute, Seattle, WA, USA.

出版信息

Blood Cells Mol Dis. 1995;21(3):192-200. doi: 10.1006/bcmd.1995.0022.

Abstract

Stimulated human peripheral blood mononuclear cells (MNC) have been shown to express both G-CSF and GM-CSF, Furthermore, G-CSF is expressed by monocytes but not lymphocytes, whereas GM-CSF is expressed largely by T lymphocytes and at low levels in monocytes/macrophages, Here we present the effect of TPA (120-O-tetradecanoyl phorbol-13-acetate) on G-CSF and GM-CSF expression in stimulated human MNCs and T lymphocytes. We observed that TPA (30nM) decreased G-CSF mRNA levels in MNCs, while ionomycin increased G-CSF in a dose-dependent manner. TPA and ionomycin individually increased GM-CSF mRNA levels in T-lymphocytes and MNCs. Further, GM-CSF was induced synergistically by TPA plus ionomycin, whereas this combination markedly decreased G-CSF mRNA levels in MNCs. These data suggest at least two signaling pathway by which G-CSF and GM-CSF and GM-CSF mRNA levels are modulated in a mixed population of monocytes and T lymphocytes, namely protein kinase C (PKC) and calcium. These signals seems to act synergistically in lymphocytes to increase GM-CSF, and not G-CSF mRNA levels specifically. It would also appear these signals act on MNCs in an opposing manner to decrease G-CSF mRNA levels, indicating that activation of PKC and the calcium signaling pathway lead to a cell-type specific modulation of individual cytokines and precise regulation of granulocyte production.

摘要

已证明受刺激的人外周血单个核细胞(MNC)可表达G-CSF和GM-CSF。此外,G-CSF由单核细胞而非淋巴细胞表达,而GM-CSF主要由T淋巴细胞表达,在单核细胞/巨噬细胞中表达水平较低。在此,我们展示了佛波酯(12-O-十四酰佛波醇-13-乙酸酯,TPA)对受刺激的人MNC和T淋巴细胞中G-CSF和GM-CSF表达的影响。我们观察到,TPA(30nM)可降低MNC中G-CSF mRNA水平,而离子霉素则以剂量依赖方式增加G-CSF。TPA和离子霉素分别增加T淋巴细胞和MNC中GM-CSF mRNA水平。此外,TPA加离子霉素可协同诱导GM-CSF,而这种组合显著降低MNC中G-CSF mRNA水平。这些数据表明,在单核细胞和T淋巴细胞混合群体中,至少有两条信号通路可调节G-CSF、GM-CSF及其mRNA水平,即蛋白激酶C(PKC)和钙信号通路。这些信号似乎在淋巴细胞中协同作用以增加GM-CSF,而非特异性增加G-CSF mRNA水平。同样,这些信号似乎以相反方式作用于MNC以降低G-CSF mRNA水平,表明PKC和钙信号通路的激活导致个体细胞因子的细胞类型特异性调节以及粒细胞生成的精确调控。

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